Canonical Allele Identifier: CA399478106

Gene: KRT14

Linked Data

• MyVariant Identifiers: chr17:g.39740568C>G (hg19) ; chr17:g.41584316C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584316C>G , CM000679.2:g.41584316C>G	GRCh38
NC_000017.10:g.39740568C>G , CM000679.1:g.39740568C>G	GRCh37
NC_000017.9:g.36994094C>G	NCBI36
NG_008624.1:g.7580G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.706G>C MANE Select	ENSP00000167586.6:p.Glu236Gln
ENST00000167586.6:c.706G>C	ENSP00000167586.6:p.Glu236Gln
ENST00000476662.1:n.156G>C
NM_000526.4:c.706G>C	NP_000517.2:p.Glu236Gln
NM_000526.5:c.706G>C MANE Select	NP_000517.3:p.Glu236Gln